A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211801



Internal ID20778841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25313021..25339859hg38UCSC Ensembl
chr4:25314643..25341481hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3826839
hg1926839
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359229
Supporting Variants
Samples
Known GenesZCCHC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211801
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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